Canonical Allele Identifier: CA2450721783

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695432A= , CM000685.2:g.108695432A=	GRCh38
NC_000023.10:g.107938662A= , CM000685.1:g.107938662A=	GRCh37
NC_000023.9:g.107825318A=	NCBI36
NG_011977.1:g.260509A=
NG_011977.2:g.260509A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4987A= MANE Select	ENSP00000331902.7:p.Met1663=
ENST00000361603.7:c.4969A=	ENSP00000354505.2:p.Met1657=
ENST00000510690.2:n.1481A=
ENST00000644079.1:n.1818A=
ENST00000328300.10:c.4987A=	ENSP00000331902.6:p.Met1663=
ENST00000361603.6:c.4969A=	ENSP00000354505.2:p.Met1657=
ENST00000504541.1:c.219+511A=	ENSP00000424845.1:n.219+511A=
ENST00000515658.1:c.325-865A=
NM_000495.4:c.4969A=	NP_000486.1:p.Met1657=
NM_033380.2:c.4987A=	NP_203699.1:p.Met1663=
XM_005262070.2:c.4978A=	XP_005262127.1:p.Met1660=
XM_006724616.2:c.4987A=	XP_006724679.1:p.Met1663=
XM_011530849.1:c.4663A=	XP_011529151.1:p.Met1555=
XM_011530851.1:c.2560A=	XP_011529153.1:p.Met854=
XM_011530849.2:c.5002A=	XP_011529151.2:p.Met1668=
XM_017029259.2:c.4993A=	XP_016884748.1:p.Met1665=
XM_017029260.1:c.4984A=	XP_016884749.1:p.Met1662=
XM_017029263.2:c.3322A=	XP_016884752.1:p.Met1108=
NM_000495.5:c.4969A=	NP_000486.1:p.Met1657=
NM_033380.3:c.4987A= MANE Select	NP_203699.1:p.Met1663=